Vxr, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vxr, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Vxr, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1983 to 1985. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Vxr, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vxr, Inc.
8 devices
Cleared
Oct 04, 1985
VENTREZYME T3 IMMUNOASSAY T3
Chemistry
30d
Cleared
Oct 01, 1985
VENTRESCREEN HCG URINE
Chemistry
22d
Cleared
May 21, 1984
VENTREXYME EIA CONTROLS IMMUNOASSAY
Immunology
42d
Cleared
Apr 04, 1984
VENTREZYME T4 IMMUNOASSAY T4
Chemistry
61d
Cleared
Feb 03, 1984
VENTREX PREGNANCY TEST KIT ENZYME
Chemistry
79d
Cleared
Jan 30, 1984
VENTREZYME THEOPHYLLINE IMMUNOASSAY
Immunology
73d
Cleared
Jan 13, 1984
VENTREZYME DIGOXIN IMMUNOASSAY DIGOX
Toxicology
66d
Cleared
Nov 21, 1983
VENTRESCREEN BETA-HCG ENZYME IMMUNO
Immunology
7d